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Analysis of the human E2 ubiquitin conjugating enzyme protein interaction network
Open accessAbstract
In eukaryotic cells the stability and function of many proteins are regulated by the addition of ubiquitin or ubiquitin-like peptides. This process is dependent upon the sequential action of an E1-activating enzyme, an E2-conjugating enzyme, and an E3 ligase. Different combinations of these proteins confer substrate specificity and the form of protein modification. However, combinatorial preferences within ubiquitination networks remain unclear. In this study, yeast two-hybrid (Y2H) screens were combined with true homology modeling methods to generate a high-density map of human E2/E3-RING interactions. These data include 535 experimentally defined novel E2/E3-RING interactions and >1300 E2/E3-RING pairs with more favorable predicted free-energy values than the canonical UBE2L3-CBL complex. The significance of Y2H predictions was assessed by both mutagenesis and functional assays. Significantly, 74/80 (>92%) of Y2H predicted complexes were disrupted by point mutations that inhibit verified E2/E3-RING interactions, and a approximately 93% correlation was observed between Y2H data and the functional activity of E2/E3-RING complexes in vitro. Analysis of the high-density human E2/E3-RING network reveals complex combinatorial interactions and a strong potential for functional redundancy, especially within E2 families that have undergone evolutionary expansion. Finally, a one-step extended human E2/E3-RING network, containing 2644 proteins and 5087 edges, was assembled to provide a resource for future functional investigations.
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“The ability of E3 ligases to interact with multiple E2 partners is supported by recent global E2-E3 interaction screens (26,27).”
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“However, some of these E2 s failed to interact with Mdm2 in another high throughput approach [26].”
From The p53 orchestra: Mdm2 and Mdmx set the tone (2010) · cites this paper as [26]
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Self-citationMiR-182-5p inhibits the tumorigenesis of clear cell renal cell carcinoma by repressing UBE2T
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Metadata
- Authors
- Markson, G., Kiel, C., Hyde, R., Brown, S., Charalabous, P., Bremm, A., Semple, J., Woodsmith, J., Duley, S., Salehi-Ashtiani, K., Vidal, M., Komander, D., Serrano, L., Lehner, P., & Sanderson, C. M.
- Affiliations
- University of Cambridge (GB)
- Institució Catalana de Recerca i Estudis Avançats (ES)
- University of Liverpool (GB)
- MRC Laboratory of Molecular Biology (GB)
- Harvard University (US)
- ORCID
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2009-06-23
- Volume
- 19
- Issue
- 10
- Pages
- 1905-1911
- ISSN
- 1088-9051 (ISSN-L)
- PMC
- PMC2765280
- OpenAlex
- W2135700703
- Cited by
- 157
- References
- 30
- Citations by year
- 2026: 3 · 2025: 2 · 2023: 5 · 2022: 8 · 2021: 4 · 2020: 10 · 2019: 3 · 2018: 11 · 2017: 7 · 2016: 12 · 2015: 19 · 2014: 6 · 2013: 17 · 2012: 18
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genome Research (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust (084957)
- Fonds De La Recherche Scientifique - FNRS
- Fédération Wallonie-Bruxelles
- Medical Research Council
- National Human Genome Research Institute (R01HG001715)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- E2 ubiquitin-conjugating enzyme, E3 ubiquitin ligase, RING domain, protein-protein interaction network, ubiquitination, yeast two-hybrid screen, homology modeling, free energy prediction, functional redundancy, human interactome
- MeSH terms
- Amino Acid Sequence, False Positive Reactions, Humans, Protein Binding, Mutagenesis, Site-Directed, Sequence Homology, Amino Acid, K562 Cells, Sequence Analysis, Protein, Two-Hybrid System Techniques, Ubiquitin-Conjugating Enzymes, Ubiquitin-Protein Ligases, Metabolic Networks and Pathways, Protein Interaction Domains and Motifs, Ubiquitination
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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